Canonical Allele Identifier: CA2649550495

Gene: HMCN1

Linked Data

• gnomAD v4: 1-185994761-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185994763_185994764del , CM000663.2:g.185994763_185994764del	GRCh38
NC_000001.10:g.185963895_185963896del , CM000663.1:g.185963895_185963896del	GRCh37
NC_000001.9:g.184230518_184230519del	NCBI36
NG_011841.1:g.265213_265214del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.3506-52_3506-51del MANE Select	ENSP00000271588.4:n.3506-52_3506-51del
ENST00000271588.8:c.3506-52_3506-51del	ENSP00000271588.4:n.3506-52_3506-51del
NM_031935.2:c.3506-52_3506-51del	NP_114141.2:n.3506-52_3506-51del
XM_011510037.1:c.3506-52_3506-51del	XP_011508339.1:n.3506-52_3506-51del
XM_011510038.1:c.3506-52_3506-51del	XP_011508340.1:n.3506-52_3506-51del
XM_011510039.1:c.3506-52_3506-51del	XP_011508341.1:n.3506-52_3506-51del
XM_011510040.1:c.3506-52_3506-51del	XP_011508342.1:n.3506-52_3506-51del
XM_011510041.1:c.3506-52_3506-51del	XP_011508343.1:n.3506-52_3506-51del
XM_011510038.3:c.3506-52_3506-51del	XP_011508340.1:n.3506-52_3506-51del
XM_011510041.3:c.3506-52_3506-51del	XP_011508343.1:n.3506-52_3506-51del
XM_017002437.1:c.1529-52_1529-51del	XP_016857926.1:n.1529-52_1529-51del
XM_024450118.1:c.3506-52_3506-51del	XP_024305886.1:n.3506-52_3506-51del
NM_031935.3:c.3506-52_3506-51del MANE Select	NP_114141.2:n.3506-52_3506-51del